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Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses

BACKGROUND: Preventing the seasonal or pandemic outbreak of influenza can be powerful and cost-effective. OBJECTIVES: In this study, we constructed a novel virus-like particle (VLP) platform that contains two hemagglutinin (HA) subtypes and evaluated immunogenicity of constructed VLP in mice. MATERI...

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Autores principales: Rezaei, Farhad, Mirshafiey, Abbas, Shahmahmoodi, Shohreh, Shoja, Zabihollah, Ghavami, Nastaran, Mokhtari-Azad, Talat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589784/
https://www.ncbi.nlm.nih.gov/pubmed/23487492
http://dx.doi.org/10.5812/ircmj.6252
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author Rezaei, Farhad
Mirshafiey, Abbas
Shahmahmoodi, Shohreh
Shoja, Zabihollah
Ghavami, Nastaran
Mokhtari-Azad, Talat
author_facet Rezaei, Farhad
Mirshafiey, Abbas
Shahmahmoodi, Shohreh
Shoja, Zabihollah
Ghavami, Nastaran
Mokhtari-Azad, Talat
author_sort Rezaei, Farhad
collection PubMed
description BACKGROUND: Preventing the seasonal or pandemic outbreak of influenza can be powerful and cost-effective. OBJECTIVES: In this study, we constructed a novel virus-like particle (VLP) platform that contains two hemagglutinin (HA) subtypes and evaluated immunogenicity of constructed VLP in mice. MATERIALS AND METHODS: This recombinant candidate vaccine model resulted in the expression of two HAs of H1N1 and H3N2 subtypes co-localized within a VLP. Following infection of insect cells with recombinant baculovirus co-expressing H1, H3 and M1 proteins, VLPs with size of 80–120 nm were self-assembled, budding, and released into the insect culture medium. The resulting VLPs which contained two different subtypes of hemagglutinin were purified by ultracentrifugation. The immunogenicity of VLPs was evaluated in mice following immunization. RESULTS: Our data showed that vaccination using VLPs elicited robust levels of serum IgG, and viral neutralizing antibodies against A/PR8 (H1N1) and A/HK (H3N2) viruses. Following challenge with lethal dose of A/PR8 (H1N1) and A/HK (H3N2, vaccinated mice were protected, displaying no sign of weight loss and mortality compared to non-vaccinated control mice. CONCLUSIONS: VLPs can serve as a promising vaccination strategy to control influenza virus.
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spelling pubmed-35897842013-03-13 Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses Rezaei, Farhad Mirshafiey, Abbas Shahmahmoodi, Shohreh Shoja, Zabihollah Ghavami, Nastaran Mokhtari-Azad, Talat Iran Red Crescent Med J Research Article BACKGROUND: Preventing the seasonal or pandemic outbreak of influenza can be powerful and cost-effective. OBJECTIVES: In this study, we constructed a novel virus-like particle (VLP) platform that contains two hemagglutinin (HA) subtypes and evaluated immunogenicity of constructed VLP in mice. MATERIALS AND METHODS: This recombinant candidate vaccine model resulted in the expression of two HAs of H1N1 and H3N2 subtypes co-localized within a VLP. Following infection of insect cells with recombinant baculovirus co-expressing H1, H3 and M1 proteins, VLPs with size of 80–120 nm were self-assembled, budding, and released into the insect culture medium. The resulting VLPs which contained two different subtypes of hemagglutinin were purified by ultracentrifugation. The immunogenicity of VLPs was evaluated in mice following immunization. RESULTS: Our data showed that vaccination using VLPs elicited robust levels of serum IgG, and viral neutralizing antibodies against A/PR8 (H1N1) and A/HK (H3N2) viruses. Following challenge with lethal dose of A/PR8 (H1N1) and A/HK (H3N2, vaccinated mice were protected, displaying no sign of weight loss and mortality compared to non-vaccinated control mice. CONCLUSIONS: VLPs can serve as a promising vaccination strategy to control influenza virus. Kowsar 2013-01-05 2013-01 /pmc/articles/PMC3589784/ /pubmed/23487492 http://dx.doi.org/10.5812/ircmj.6252 Text en Copyright © 2013, Iranian Red Crescent Medical Journal http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rezaei, Farhad
Mirshafiey, Abbas
Shahmahmoodi, Shohreh
Shoja, Zabihollah
Ghavami, Nastaran
Mokhtari-Azad, Talat
Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
title Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
title_full Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
title_fullStr Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
title_full_unstemmed Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
title_short Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
title_sort influenza virus-like particle containing two different subtypes of hemagglutinin confers protection in mice against lethal challenge with a/pr8 (h1n1) and a/hk (h3n2) viruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589784/
https://www.ncbi.nlm.nih.gov/pubmed/23487492
http://dx.doi.org/10.5812/ircmj.6252
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